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U.S. Department of Health and Human Services

Medical Device Recalls
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21 to 28 of 28 Results
Related Medical Device Recalls
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Z-1340-2008 - Implantable Cardioverter Defibrillator ATLAS + HF Tiered-therapy cardioverter/defibrillator with biventricular stimulation, Model V-340 2 08/19/2008 St Jude Medical CRMD
Z-1341-2008 - Implantable Cardioverter Defibrillator ATLAS + HF Tiered-therapy cardioverter/defibrillator with biventricular stimulation, Model V-343 2 08/19/2008 St Jude Medical CRMD
Z-1342-2008 - Implantable Cardioverter Defibrillator ATLAS II VR Tiered-therapy cardioverter/defibrillator, Model V-168 2 08/19/2008 St Jude Medical CRMD
Z-1343-2008 - Implantable Cardioverter Defibrillator ATLAS II DR Tiered-therapy cardioverter/defibrillator, Model V-265 2 08/19/2008 St Jude Medical CRMD
Z-1344-2008 - Implantable Cardioverter Defibrillator ATLAS II+ DR Tiered-therapy cardioverter/defibrillator, Model V-268 2 08/19/2008 St Jude Medical CRMD
Z-1345-2008 - Implantable Cardioverter Defibrillator ATLAS II HF Tiered-therapy cardioverter/defibrillator with biventricular stimulation, Model V-365 2 08/19/2008 St Jude Medical CRMD
Z-1346-2008 - Implantable Cardioverter Defibrillator ATLAS II+ HF Tiered-therapy cardioverter/defibrillator with biventricular stimulation, Model V-366 2 08/19/2008 St Jude Medical CRMD
Z-1321-2008 - Implantable Cardioverter Defibrillator EPIC DR Tiered-Therapy Cardioverter/Defibrillator, Model V-235 2 08/19/2008 St Jude Medical CRMD
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